Canonical Allele Identifier: PA2825617064
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2125367
ClinVar RCV Id: RCV003049541
ClinVar Variation Id: 2702402
ClinVar RCV Id: RCV003510559
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Phe74Leu
CA397844490
NM_001126118.1:c.222C>G
CA397844493
NM_001126118.1:c.222C>A
CA397844508
NM_001126118.1:c.220T>C